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1.What is the beta-Diphosphopyridine nucleotide ?
β-Nicotinamide Adenine Dinucleotide is a coeznyme consisting of an adenine base and a nicotinamide base connected by a pair of bridging phosphate group. β-Nicotinamide Adenine Dinucleotide acts as a c oenzyme in redox reactions, as a donor of ADP-ribose moieties in ADP-ribosylation reactions and also as a precursor of the second messenger molecule cyclic ADP-ribose. β-Nicotinamide Adenine Dinucleot ide also acts as a substrate for bacterial DNA ligases and a group of enzymes called sirtuins that use NAD+ to remove acetyl groups from proteins.
Conditions
| Conditions |
Yield |
|
With
oxygen;
coenzyme PQQ;
In
water;
at 30 ℃;
Rate constant;
pH 6.7; other catalysts, without and with diaphorase;
|
|
|
With
oxygen;
In
water;
at 25 ℃;
Mechanism;
Irradiation;
biochemical oscillator with horseradish peroxidase; effect of light, role of methylene blue added; pH 5.10 (sodium acetate buffer);
|
|
|
With
oxygen;
In
water;
at 25 ℃;
Mechanism;
biochemical oscillator with horseradish peroxidase; effects of catalase and superoxide dismutase enzymes added, roles of hydrogen peroxide and methylene blue added; pH 5.10 (sodium acetate buffer);
|
|
|
With
α1P2W17VO628-; buffer pH=7;
In
water;
at 20 ℃;
under 760 Torr;
Mechanism;
Rate constant;
|
|
|
With
oxygen;
diaphorase; pyrroloquinoline quinone;
In
water;
at 30 ℃;
pH 6.7;
|
|
|
With
mercury dichloride;
In
water;
at 20 ℃;
pH=7.4;
Further Variations:;
Reagents;
Kinetics;
|
|
|
With
4-oxo-TPO; Nitrite; Nitrogen dioxide;
In
phosphate buffer;
pH=6.8;
Kinetics;
ambient temperature;
|
|
|
With
poly(aniline)-poly(vinyl sulfonate) modified electrode;
In
various solvent(s);
at 25 ℃;
pH=7.0;
Kinetics;
Electrochemical reaction;
|
|
|
With
flavocytochrome P450 BM3 wild type;
In
various solvent(s);
at 15 ℃;
pH=7.0;
Further Variations:;
Reagents;
Enzyme kinetics;
|
|
|
Fe3O4-[3-(2-aminoethyl)aminopropyl]trimethoxysilane-PQQ;
In
various solvent(s);
pH=7.0;
Kinetics;
Electrochemical reaction;
|
|
|
With
poly(aniline)-poly(acrylate) film;
In
various solvent(s);
at 25 ℃;
Further Variations:;
potentials; film thicknesses;
Kinetics;
Electrochemical reaction;
|
|
|
With
sfnoxK2 NADH oxidase from Lactobacillus sanfranciscensis; oxygen;
In
various solvent(s);
at 30 ℃;
pH=7;
Further Variations:;
Reagents;
Kinetics;
Enzyme kinetics;
Enzymatic reaction;
|
|
|
With
Bacillus subtilis nitroreductase NfrA1; oxygen; ammonium bicarbonate;
In
water;
at 37 ℃;
pH=8.4;
Enzymatic reaction;
|
|
|
With
human recombinant 3β-hydroxysteroid dehydrogenase/Delta 5->4 isomerase type 2; 5-androstenedione;
at 27 ℃;
pH=7.4;
Concentration;
Reagent/catalyst;
Kinetics;
aq. phosphate buffer;
|
|
|
With
Thermus thermophilus lactate dehydrogenase A75G mutant; sodium pyruvate; magnesium chloride;
at 25 ℃;
pH=7.5;
Concentration;
Reagent/catalyst;
Temperature;
Kinetics;
aq. buffer;
Enzymatic reaction;
|
|
|
With
sodium hydroxide;
C20H24IrN2O3(1+)*0.5O4S(2-);
In
water; acetonitrile;
at 25 ℃;
Conversion of starting material;
|
|
|
NADH;
With
1-(4-hydroxy-3,5-dimethoxy-phenyl)-ethanone; triethylamine;
In
aq. acetate buffer;
at 30 ℃;
for 0.0833333h;
pH=7;
With
laccase from Myceliophthora thermophila;
In
aq. acetate buffer;
Reagent/catalyst;
pH-value;
Catalytic behavior;
Kinetics;
Enzymatic reaction;
|
|
|
With
laccase from Myceliophthora thermophilia; oxygen; methylene blue;
In
aq. buffer;
at 30 ℃;
pH=7;
Reagent/catalyst;
Time;
Catalytic behavior;
Irradiation;
Enzymatic reaction;
|
|
|
With
[(η5-pentamethylcyclopentadienyl)Ir(2-(4-hydroxyphenyl)pyridine)Cl];
In
methanol; aq. phosphate buffer;
at 36.84 ℃;
for 24h;
pH=7.5;
Reagent/catalyst;
Concentration;
Catalytic behavior;
|
|
|
With
reduced flavin mononucleotide;
In
aq. phosphate buffer;
at 30 ℃;
pH=7;
Reagent/catalyst;
Wavelength;
Catalytic behavior;
Schlenk technique;
Irradiation;
|
|
|
With
[(η5-C5Me4C6H4C6H5)Ir(2,6-diisopropyl-N-(quinolin-2-ylmethylene)aniline)Cl]PF6;
In
methanol; water;
at 24.84 ℃;
for 7.5h;
Solvent;
Reagent/catalyst;
Temperature;
Time;
|
|
|
With
alcohol dehydrogenase from Saccharomyces cerevisiae; acetaldehyde;
Enzymatic reaction;
|
|
|
With
C32H42ClO3PRuS;
In
methanol; water;
at 24.84 ℃;
for 8h;
Reagent/catalyst;
Temperature;
Solvent;
|
|
|
With
C37H41ClIrN4(1+)*Cl(1-);
In
methanol; water;
at 24.84 ℃;
for 7h;
Kinetics;
|
|
|
With
[(η5‐1,2,3,4,5‐pentamethyl‐cyclopentadiene)Ir(1,2‐bis(diphenylphosphino)ethane)Cl]hexafluorophosphate;
In
methanol; water;
at 24.84 ℃;
for 8h;
Catalytic behavior;
UV-irradiation;
|
|
|
With
1,4-dithio-D,L-threitol; NADH oxidase immobilized onto PureCube Ni-IDA MagBeads;
In
aq. buffer;
pH=6.5;
Catalytic behavior;
Kinetics;
Enzymatic reaction;
|
|
|
With
C33H33ClFeIrN;
In
methanol; water;
at 24.84 ℃;
for 8h;
Reagent/catalyst;
Catalytic behavior;
|
|
|
With
Mycobacterium smegmatis carveol dehydrogenase; 5-[(p-hydroxyphenyl)methyl]-4,4-dimethyl-2,3-pyrrolidinedione;
Enzymatic reaction;
|
|
|
With
oxygen; [(4,4'-di-tert-butyl-2,2'-bipyridine)2Ru(dipyrido[3,2-a:2’,3’-c]phenazine)]Cl2;
In
water;
for 2h;
Reagent/catalyst;
Catalytic behavior;
Irradiation;
Sealed tube;
|
|
-
-
1094-61-7
nicotinamide mononucleotide
-
-
24558-92-7
N,N'-dicyclohexyl-4-morpholinecarboxamidinium salt of adenosine-5'-phosphoromorpholidate
Conditions
| Conditions |
Yield |
|
With
magnesium sulfate; manganese(ll) chloride;
In
formamide;
for 16h;
Ambient temperature;
|
58%
|
2.What is the CAS number for beta-Diphosphopyridine nucleotide ?
The CAS number of beta-Diphosphopyridine nucleotide is 53-84-9.
More information of beta-Diphosphopyridine nucleotide 53-84-9 are:
|
CAS Number
|
53-84-9 |
|
Melting Point
|
140 - 142oC |
|
HS CODE
|
29349990 |
|
PSA
|
340.71000 |
|
LogP
|
-1.29620 |
3.What are another words for beta-Diphosphopyridine nucleotide ?
Synonyms for beta-Diphosphopyridine nucleotide 53-84-9:5'-ester with 3-(aminocarbonyl)-1-b-D-ribofuranosylpyridinium hydroxide, inner salt;Adenine-nicotinamide dinucleotide;CO-I;Codehydrase I;Codehydrogenase I;Coenzyme I;Cozymase I;DPN;Diphosphopyridine nucleotide;Enzopride;NAD;NAD+;NSC 20272;Nadide;Nicotinamide-adenine dinucleotide;Oxidized diphosphopyridine nucleotide;Adenosine5'-(trihydrogen diphosphate), P'?5'-ester with 3-(aminocarbonyl)-1-b-D-ribofuranosylpyridinium, inner salt;b-NAD;b-NAD+;b-Nicotinamide adenine dinucleotide;[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl [[(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-oxido-phosphoryl] phosphate;
4.What is the molecular formula of beta-Diphosphopyridine nucleotide?
The chemical formula of beta-Diphosphopyridine nucleotide is C21H27N7O14P2 which containing 21 Carbon atoms,27 Hydrogen atoms,7 Nitrogen atoms,14 Oxygen atoms and 2 Phosphorus atoms,and the molecular weight of beta-Diphosphopyridine nucleotide is 663.431.
5.What is beta-Diphosphopyridine nucleotide (53-84-9) used for?
β-Nicotinamide adenine dinucleotide (NAD+) plays a major role in metabolism as a cofactor and mobile electron acceptor. NAD+ is a required oxidizing cosubstrate for many enzymes. It is reduced to NADH (Cat# N-035) which carries electrons to the electron transport chain for subsequent oxidative phorphorylation and ATP production. NAD+ is capable of donating ADP-ribose moieties to a protein, producing nicotinamide in the process. Sirtuin enzymes use NAD+ as a substrate to deacetylate proteins and direct activity between the nucleus and mitochondria. NAD+ is regenerated by fermentation and by oxidative phosphorylation.
InChI:InChI=1/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/p-1/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
Relevant articles related to beta-Diphosphopyridine nucleotide:
|
Article
|
Source
|
|
The Role of Adsorption in the Initial One-Electron Electrochemical Reduction of Nicotinamide Adenine Dinucleotide (NAD+)
|
Bresnahan, William T.,Elving, Philip J.
, p. 2379 - 2386 (1981)
|
|
Synthesis of Nicotinamide Adenine Dinucleotide (NAD) from Adenosine Monophosphate (AMP)
|
Walt, David R.,Rios-Mercadillo, Victor M.,Auge, Jacques,Whitesides, George M.
, p. 7805 - 7806 (1980)
|
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